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  4. NDC Product Code: 51367-019 Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster

NDC 51367-019 Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51367-019?
  4. Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51367-019
Proprietary Name:
Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Nature Nutraceuticals
Labeler Code:
51367
Product Label ID:
df0e307f-8612-4bb2-bee3-a91f1b2ab1ba
Start Marketing Date: [9]
08-01-1991
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 51367-019?

The NDC code 51367-019 is assigned by the FDA to the product Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster which is product labeled by International Nature Nutraceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51367-019-10 10 plaster in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster?

Adults and Children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 12 hoursChildren 2 to 12 years of age and adults with compromised health: use only the guidance of a doctorChildren under 2 years of age: do not use

Which are Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".